Allele Registry

Canonical Allele Identifier: PA2830171629

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000458972

RCV000566191

RCV003392264

ClinVar Variation:

403821

HGVS (amino-acid)	Matching Registered Transcripts
NP_570711.2:p.Lys502Asn	CA060705 NM_130799.3:c.1506G>C CA381178780 NM_130799.3:c.1506G>T